NCCN Clinical Practice Guidelines: Systemic Mastocytosis

NCCN Clinical Practice Guidelines: Systemic Mastocytosis

Updates to Treatment Protocols

  1. Second-Line Therapy for Bone Pain
    • For patients unresponsive to bisphosphonates or those with renal insufficiency contraindicated for bisphosphonates, ‌anti-RANKL monoclonal antibodies (e.g., denosumab)‌ are recommended. FDA-approved biosimilars are suitable alternatives.
  2. Additions for Indolent and Smoldering Subtypes
    • For ‌indolent systemic mastocytosis (ISM)‌ and ‌smoldering systemic mastocytosis (SSM)‌, ‌cladribine‌ or ‌peginterferon alfa-2a‌ is added as “potentially beneficial in select cases.”
  3. Adjustments for Aggressive Subtypes
    • For ‌aggressive systemic mastocytosis (ASM)‌, ‌systemic mastocytosis with associated hematologic neoplasm (SM-AHN)‌, and ‌mast cell leukemia (MCL) ± AHN‌:
      • If clinical benefit fails to meet the 2013 IWG-MRT-ECNM response criteria, restage the disease, consider ‌second-line multiagent chemotherapy‌, and evaluate eligibility for ‌allogeneic hematopoietic cell transplantation (HCT)‌.
  4. Removal of Toxicity Management Content
    • Sections on ‌avapritinib‌ and ‌midostaurin‌ toxicity management were removed.

Treatment Recommendations by Subtype

  1. Symptomatic ISM or SSM
    • First-line:‌ Mediator-targeting therapies for symptom control; clinical trial enrollment is preferred.
    • Avapritinib‌ is recommended for symptomatic ISM patients with ‌platelet count ≥50 × 10⁹/L‌.
    • Cladribine‌ or ‌peginterferon alfa-2a‌ may be used in severe, refractory cases with mediator-related symptoms or bone disease.
  2. ASM, SM-AHN (SM-dominant), and MCL (with/without AHN)
    • First-line:‌ Clinical trials, ‌avapritinib‌ (platelet count ≥50 × 10⁹/L), or ‌midostaurin‌.
    • Other options:‌ Cladribine, peginterferon alfa-2a (± prednisone).
    • Imatinib‌ is reserved for rare cases (e.g., KIT D816V-negative/unknown ASM, FIP1L1::PDGFRA fusion-associated eosinophilia).

Drug Efficacy and Safety

  1. Avapritinib
    • In trials: Significant reduction in total symptom score, serum tryptase, and KIT D816V allele burden after 24 weeks in moderate-severe ISM.
    • ORR:‌ 75% in advanced SM.
    • Safety:‌ Comparable grade ≥3 adverse events (AEs) to placebo (e.g., flushing, peripheral edema). Prolongs median overall survival.
  2. Midostaurin
    • ORR:‌ 60% in 116 advanced SM patients, consistent across subtypes.
    • AEs:‌ Low-grade nausea/vomiting/diarrhea; grade 3–4 cytopenias (neutropenia, anemia, thrombocytopenia).
  3. Cladribine
    • ORR:‌ 56% (ISM), 50% (ASM), 55% (SM-AHN). Reduces mast cell metabolites and marrow burden.
    • AEs:‌ Grade 3–4 lymphopenia, neutropenia, opportunistic infections.

Allogeneic Hematopoietic Cell Transplantation (HCT)

  • Retrospective data (pre-KIT inhibitor era) from 57 advanced SM patients:
    • ORR:‌ 70% post-HCT.
    • 3-year OS:‌ 74% (SM-AHN), 43% (ASM), 17% (MCL).
    • Key risk factor:‌ MCL subtype predicts poor survival.
  • Prospective trials are needed to clarify HCT’s role in advanced SM.

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